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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:195600 - decan-2-ol
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ChEBI Ontology
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ChEBI Name
decan-2-ol
ChEBI ID
CHEBI:195600
Definition
A secondary alcohol that is decane substituted by a hydroxy group at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C10H22O
Net Charge
0
Average Mass
158.285
Monoisotopic Mass
158.16707
InChI
InChI=1S/C10H22O/c1-3-4-5-6-7-8-9-10(2)11/h10-11H,3-9H2,1-2H3
InChIKey
ACUZDYFTRHEKOS-UHFFFAOYSA-N
SMILES
CCCCCCCCC(C)O
Metabolite of Species
Details
Paenibacillus polymyxa
(NCBI:txid1406)
of strain KM2501-1 See:
PubMed
Meccus pallidipennis
(NCBI:txid30077)
Species also known as Triatoma pallidipennis. See:
PubMed
Tetanops myopaeformis
(NCBI:txid454641)
See:
PubMed
Roles Classification
Biological Role
(s):
animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Application
(s):
nematicide
A substance used to destroy pests of the phylum
Nematoda
(roundworms).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
decan-2-ol (
CHEBI:195600
)
has role
animal metabolite (
CHEBI:75767
)
decan-2-ol (
CHEBI:195600
)
has role
bacterial metabolite (
CHEBI:76969
)
decan-2-ol (
CHEBI:195600
)
has role
nematicide (
CHEBI:25491
)
decan-2-ol (
CHEBI:195600
)
is a
decanol (
CHEBI:195598
)
decan-2-ol (
CHEBI:195600
)
is a
secondary alcohol (
CHEBI:35681
)
IUPAC Name
decan-2-ol
Synonyms
Sources
1-methyl-1-nonanol
ChEBI
1-methylnonyl alcohol
ChEBI
2-decanol
ChEBI
2-decyl alcohol
ChEBI
2-hydroxydecane
ChEBI
methyl-
n
-octyl carbinol
NIST Chemistry WebBook
methyl-
n
-octylcarbinol
ChEBI
Manual Xrefs
Databases
FDB007666
FooDB
HMDB0303078
HMDB
View more database links
Registry Numbers
Types
Sources
1120-06-5
CAS Registry Number
NIST Chemistry WebBook
1719664
Reaxys Registry Number
Reaxys
Citations
Types
Sources
2033592
PubMed citation
Europe PMC
27711776
PubMed citation
Europe PMC
28423428
PubMed citation
Europe PMC
29176679
PubMed citation
Europe PMC
29454375
PubMed citation
Europe PMC
8158169
PubMed citation
Europe PMC
Last Modified
23 August 2023